Linked Data
gnomAD v4:
17-42404758-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42404762del , CM000679.2:g.42404762del | GRCh38 |
| NC_000017.10:g.40556780del , CM000679.1:g.40556780del | GRCh37 |
| NC_000017.9:g.37810306del | NCBI36 |
| NG_015845.1:g.23562del | |
| NG_015845.2:g.23562del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357037.6:c.1101del MANE Select | ENSP00000349541.4:p.Asp368ThrfsTer? | |
| ENST00000357037.5:c.1101del | ENSP00000349541.4:p.Asp368ThrfsTer? | |
| NM_012232.5:c.1101del | NP_036364.2:p.Asp368ThrfsTer? | |
| NM_012232.6:c.1101del MANE Select | NP_036364.2:p.Asp368ThrfsTer? |